| | LOC126860438, LOC126860439 +3663 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC105379224, LOC105379230 +3657 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC129999966, LOC129999967 +3111 more | Copy number gain | See cases | |
| | LOC126860489, LOC126860490 +1963 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126860535, LOC126860536 +1687 more | Copy number gain | See cases | |
| | LOC105375713, LOC105375742 +1553 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130001109, LOC130001110 +1532 more | Copy number gain | See cases | |
| | LOC130001226, LOC130001227 +1407 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130000987, LOC130000988 +1205 more | Copy number gain | See cases | |
| | LOC130001173, LOC130001174 +1068 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC130001070, LOC130001071 +962 more | Copy number gain | See cases | |
| | LOC130001241, LOC130001242 +559 more | Copy number gain | Neurodevelopmental disorder | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | C8orf76, ZHX1-C8orf76 (A154P +1 more) | Single nucleotide variant (missense variant) | not specified | |
| | C8orf76, ZHX1-C8orf76 (F8V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (R866W) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (K793R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (R761T) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (R757C) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (R751W) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (G746E) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (P656R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (A655S) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (D651G) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (V592A) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (N589Y) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (E545G) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (T504M) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (M498T) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (S492L) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (H490R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (Q451R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (P442L) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (T437A) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (A434T) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | EBV-positive nodal T- and NK-cell lymphoma | |
| | ZHX1, ZHX1-C8orf76 (A319T) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (M311V) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (N284S) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (V279I) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (P244T) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (I238V) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (S235G) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (E231D) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (P216R) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (V171I) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (N162Y) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (V158I) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (I148V) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | ZHX1, ZHX1-C8orf76 (R138H) | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +2 more) | not specified | |
| | | Copy number loss | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number loss | Exostoses, multiple, type 1 | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Polydactyly | |
| | | Copy number gain | not provided | |
| | DCAF4L2, DCSTAMP +333 more | Copy number gain | not specified | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | | Deletion | Trichorhinophalangeal dysplasia type I | |
| | | Copy number gain | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | SLC45A4, SLC7A13 +189 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |